Academic literature on the topic 'Enhancers RNAs'

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Journal articles on the topic "Enhancers RNAs"

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Hah, Nasun, Chris Benner, Ling-Wa Chong, Ruth T. Yu, Michael Downes, and Ronald M. Evans. "Inflammation-sensitive super enhancers form domains of coordinately regulated enhancer RNAs." Proceedings of the National Academy of Sciences 112, no. 3 (2015): E297—E302. http://dx.doi.org/10.1073/pnas.1424028112.

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Enhancers are critical genomic elements that define cellular and functional identity through the spatial and temporal regulation of gene expression. Recent studies suggest that key genes regulating cell type-specific functions reside in enhancer-dense genomic regions (i.e., super enhancers, stretch enhancers). Here we report that enhancer RNAs (eRNAs) identified by global nuclear run-on sequencing are extensively transcribed within super enhancers and are dynamically regulated in response to cellular signaling. Using Toll-like receptor 4 (TLR4) signaling in macrophages as a model system, we fi
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de Lara, Josué Cortés-Fernández, Rodrigo G. Arzate-Mejía, and Félix Recillas-Targa. "Enhancer RNAs: Insights Into Their Biological Role." Epigenetics Insights 12 (January 2019): 251686571984609. http://dx.doi.org/10.1177/2516865719846093.

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Enhancers play a central role in the transcriptional regulation of metazoans. Almost a decade ago, the discovery of their pervasive transcription into noncoding RNAs, termed enhancer RNAs (eRNAs), opened a whole new field of study. The presence of eRNAs correlates with enhancer activity; however, whether they act as functional molecules remains controversial. Here we review direct experimental evidence supporting a functional role of eRNAs in transcription and provide a general pipeline that could help in the design of experimental approaches to investigate the function of eRNAs. We propose th
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Lewis, Michael W., Shen Li, and Hector L. Franco. "Transcriptional control by enhancers and enhancer RNAs." Transcription 10, no. 4-5 (2019): 171–86. http://dx.doi.org/10.1080/21541264.2019.1695492.

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Kim, Tae-Kyung, Martin Hemberg, and Jesse M. Gray. "Enhancer RNAs: A Class of Long Noncoding RNAs Synthesized at Enhancers: Figure 1." Cold Spring Harbor Perspectives in Biology 7, no. 1 (2015): a018622. http://dx.doi.org/10.1101/cshperspect.a018622.

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Higgs, Douglas. "Regulated RNA Expression and Normal Erythropoiesis." Blood 124, no. 21 (2014): SCI—34—SCI—34. http://dx.doi.org/10.1182/blood.v124.21.sci-34.sci-34.

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Although a small number of the vast array of long non-coding RNAs (lncRNAs) have known effects on cellular processes, in general their contribution to development, differentiation and disease remains unknown. We have shown that some intragenic enhancers, when active, behave as alternative promoters producing lncRNA transcripts that are processed using the canonical signals of their host gene. More recently we have also analyzed intergenic lncRNAs to determine the extent to which they too might originate from intergenic enhancers. We find that intergenic lncRNAs in erythroid cells are almost ev
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Ibragimov, Airat N., Oleg V. Bylino, and Yulii V. Shidlovskii. "Molecular Basis of the Function of Transcriptional Enhancers." Cells 9, no. 7 (2020): 1620. http://dx.doi.org/10.3390/cells9071620.

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Transcriptional enhancers are major genomic elements that control gene activity in eukaryotes. Recent studies provided deeper insight into the temporal and spatial organization of transcription in the nucleus, the role of non-coding RNAs in the process, and the epigenetic control of gene expression. Thus, multiple molecular details of enhancer functioning were revealed. Here, we describe the recent data and models of molecular organization of enhancer-driven transcription.
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Ørom, Ulf Andersson, and Ramin Shiekhattar. "Long non-coding RNAs and enhancers." Current Opinion in Genetics & Development 21, no. 2 (2011): 194–98. http://dx.doi.org/10.1016/j.gde.2011.01.020.

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Xu, Liang, Ye Chen, Yulun Huang, et al. "Topography of transcriptionally active chromatin in glioblastoma." Science Advances 7, no. 18 (2021): eabd4676. http://dx.doi.org/10.1126/sciadv.abd4676.

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Molecular profiling of the most aggressive brain tumor glioblastoma (GBM) on the basis of gene expression, DNA methylation, and genomic variations advances both cancer research and clinical diagnosis. The enhancer architectures and regulatory circuitries governing tumor-intrinsic transcriptional diversity and subtype identity are still elusive. Here, by mapping H3K27ac deposition, we analyze the active regulatory landscapes across 95 GBM biopsies, 12 normal brain tissues, and 38 cell line counterparts. Analyses of differentially regulated enhancers and super-enhancers uncovered previously unre
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Esse, Ruben, and Alla Grishok. "Caenorhabditis elegans Deficient in DOT-1.1 Exhibit Increases in H3K9me2 at Enhancer and Certain RNAi-Regulated Regions." Cells 9, no. 8 (2020): 1846. http://dx.doi.org/10.3390/cells9081846.

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The methylation of histone H3 at lysine 79 is a feature of open chromatin. It is deposited by the conserved histone methyltransferase DOT1. Recently, DOT1 localization and H3K79 methylation (H3K79me) have been correlated with enhancers in C. elegans and mammalian cells. Since earlier research implicated H3K79me in preventing heterochromatin formation both in yeast and leukemic cells, we sought to inquire whether a H3K79me deficiency would lead to higher levels of heterochromatic histone modifications, specifically H3K9me2, at developmental enhancers in C. elegans. Therefore, we used H3K9me2 Ch
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Carullo, Nancy V. N., Robert A. Phillips III, Rhiana C. Simon, et al. "Enhancer RNAs predict enhancer–gene regulatory links and are critical for enhancer function in neuronal systems." Nucleic Acids Research 48, no. 17 (2020): 9550–70. http://dx.doi.org/10.1093/nar/gkaa671.

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Abstract Genomic enhancer elements regulate gene expression programs important for neuronal fate and function and are implicated in brain disease states. Enhancers undergo bidirectional transcription to generate non-coding enhancer RNAs (eRNAs). However, eRNA function remains controversial. Here, we combined Assay for Transposase-Accessible Chromatin using Sequencing (ATAC-Seq) and RNA-Seq datasets from three distinct neuronal culture systems in two activity states, enabling genome-wide enhancer identification and prediction of putative enhancer–gene pairs based on correlation of transcription
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Dissertations / Theses on the topic "Enhancers RNAs"

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Chen, Li. "Functional and evolutionary characterization of flowering-related long non-coding RNAs." Doctoral thesis, Humboldt-Universität zu Berlin, 2021. http://dx.doi.org/10.18452/22833.

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Genomweite Bemühungen haben eine große Anzahl langer nichtkodierender RNAs (lncRNAs) identifiziert, obwohl ihre möglichen Funktionen weitgehend rätselhaft bleiben. Hier verwendeten wir ein System zur synchronisierten Blüteninduktion in Arabidopsis, um 4106 blütenbezogene lange intergene RNAs (lincRNAs) zu identifizieren. Blütenbezogene lincRNAs sind typischerweise mit funktionellen Enhancern assoziiert, die bidirektional transkribiert werden und mit verschiedenen funktionellen Genmodulen assoziiert sind, die mit der Entwicklung von Blütenorganen zusammenhängen, die durch Koexpressionsnetzwerka
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Zhuang, Jimmy Jiajia. "Phenotypes and genetic mechanisms of C. elegans enhanced RNAi." Thesis, Harvard University, 2013. http://dissertations.umi.com/gsas.harvard:10758.

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RNA interference (RNAi) potently and specifically induces gene knockdown, and its potential for reverse genetics in Caenorhabditis elegans is enormous. However, even in these nematodes, RNAi can be induced more effectively via enhanced RNAi (Eri) mutant backgrounds. With advances in small RNA sequencing, evidence has suggested that the eri pathway plays an endogenous gene regulatory role, which competes with experimentally introduced RNAi triggers for limiting resources. However, the nature, cellular location, and physiological consequences of this small RNA pathways competition remain unclear
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Neugebauer, Karla M., Inna Grishina, Anita S. Bledau, and Imke Listerman. "Extragenic Accumulation of RNA Polymerase II Enhances Transcription by RNA Polymerase III." PLOS, 2007. https://tud.qucosa.de/id/qucosa%3A27951.

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Recent genomic data indicate that RNA polymerase II (Pol II) function extends beyond conventional transcription of primarily protein-coding genes. Among the five snRNAs required for pre-mRNA splicing, only the U6 snRNA is synthesized by RNA polymerase III (Pol III). Here we address the question of how Pol II coordinates the expression of spliceosome components, including U6. We used chromatin immunoprecipitation (ChIP) and high-resolution mapping by PCR to localize both Pol II and Pol III to snRNA gene regions. We report the surprising finding that Pol II is highly concentrated ∼300 bp upstrea
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Neugebauer, Karla M., Inna Grishina, Anita S. Bledau, and Imke Listerman. "Extragenic Accumulation of RNA Polymerase II Enhances Transcription by RNA Polymerase III." Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-184076.

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Recent genomic data indicate that RNA polymerase II (Pol II) function extends beyond conventional transcription of primarily protein-coding genes. Among the five snRNAs required for pre-mRNA splicing, only the U6 snRNA is synthesized by RNA polymerase III (Pol III). Here we address the question of how Pol II coordinates the expression of spliceosome components, including U6. We used chromatin immunoprecipitation (ChIP) and high-resolution mapping by PCR to localize both Pol II and Pol III to snRNA gene regions. We report the surprising finding that Pol II is highly concentrated ∼300 bp upstrea
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Caglio, Giulia. "RNA Polymerase II identifies enhancers in different states of activation." Doctoral thesis, Humboldt-Universität zu Berlin, 2019. http://dx.doi.org/10.18452/19946.

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Enhancer regulieren die Transkription ihrer Zielgene und deren Expression. Sie bieten eine Bindestelle für verschiedenste Transkriptionsfaktoren (TF) und RNA Polymerase II (RNAPII) und unterstützen die Gentranskription durch das Zustandekommen von Chromatinkontakten. Zusätzlich transkribiert RNAPII in Enhancer-Regionen kurze, non-polyadenylierte Transkripte, die man Enhancer-RNA (eRNA) nennt. Der Mechanismus der RNAPII-Rekrutierung und –Regulation an Enhancern ist bisher wenig verstanden, insbesondere wie das Vorhandensein von RNAPII-Modifikationen den Chromatinstatus, -faltung sowie die Genak
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Ribeiro, Mariana Martins 1984. "G-quadruplex formation enhances splicing efficiency of PAX9 intron 1." [s.n.], 2014. http://repositorio.unicamp.br/jspui/handle/REPOSIP/290066.

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Orientadores: Sérgio Roberto Peres Line, Marcelo Rocha Marques<br>Texto em português e inglês<br>Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Odontologia de Piracicaba<br>Made available in DSpace on 2018-08-24T17:45:16Z (GMT). No. of bitstreams: 1 Ribeiro_MarianaMartins_D.pdf: 2903322 bytes, checksum: 9e0e5e91a22262495ca9bf8ae1d84cec (MD5) Previous issue date: 2014<br>Resumo: G-Quadruplexes são estruturas secundárias presentes nas moléculas de DNA e RNA, os quais são formados pelo empilhamento de G-quartetos (interação de quatro guaninas (G-tratos) delimitadas por ligaç
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Hughes, Amanda Dawn. "Mechanism of enhancer-dependent transcription in Escherichia coli by σⁿ-RNA polymerase." Thesis, University of York, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.399583.

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Scionti, Isabella. "Epigenetic Regulation of Skeletal Muscle Differentiation." Thesis, Lyon, 2017. http://www.theses.fr/2017LYSEN084/document.

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LSD1 et PHF2 sont des déméthylases de lysines capables de déméthyler à la fois les protéines histones qui influencent l’expression génique et les protéines non histones en affectant leurs activités ou stabilités. Des approches fonctionnelles d’inactivation de Lsd1 ou Phf2 chez la souris ont démontré l’implication de ces enzymes dans l'engagement des cellules progénitrices au cours de la différenciation. La myogenèse est l'un des exemples les mieux caractérisés sur la façon dont les cellules progénitrices se multiplient et se différencient pour former un organe fonctionnel. Elle est initiée par
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Robinson, Robert Maxwell. "Splicing signals in Caenorhabditis elegans : candidate exonic splicing enhancer motifs /." Thesis, Connect to this title online; UW restricted, 2005. http://hdl.handle.net/1773/10846.

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Donald, Claire Louisa. "Development of molecular tools to enhance understanding of antiviral RNAi in mosquitoes." Thesis, University of Glasgow, 2015. http://theses.gla.ac.uk/6207/.

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Mosquito-borne arboviruses are a considerable threat to human and animal health across the world. Many of them are classed as emerging or remerging pathogens and the incidence of disease for a number of serious viral infections has increased as they expand their geographical and host ranges. As with other invertebrates, mosquitoes lack the adaptive immune response present in vertebrates and instead rely on their innate immune defences to modulate viral infections. Nevertheless, in contrast to vertebrates, arboviral infections in their arthropod vector are non-pathogenic and have no cytopathic
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Books on the topic "Enhancers RNAs"

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Ørom, Ulf Andersson, ed. Enhancer RNAs. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-4035-6.

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Therapeutic Oligonucleotides: Antisense, Rnai, Triple-Helix, Gene Repair, Enhancer Decoys, Cpg, and DNA Chips (Annals of the New York Academy of Sciences). New York Academy of Sciences, 2003.

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(Editor), Alan M. Gewirtz, ed. Therapeutic Oligonucleotides: Antisense, Rnai, Triple-Helix, Gene Repair, Enhancer Decoys, Cpg, and DNA Chips (Annals of the New York Academy of Sciences). New York Academy of Sciences, 2004.

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Schadt, Eric E. Network Methods for Elucidating the Complexity of Common Human Diseases. Edited by Dennis S. Charney, Eric J. Nestler, Pamela Sklar, and Joseph D. Buxbaum. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190681425.003.0002.

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The life sciences are now a significant contributor to the ever expanding digital universe of data, and stand poised to lead in both the generation of big data and the realization of dramatic benefit from it. We can now score variations in DNA across whole genomes; RNA levels and alternative isoforms, metabolite levels, protein levels, and protein state information across the transcriptome, metabolome and proteome; methylation status across the methylome; and construct extensive protein–protein and protein–DNA interaction maps, all in a comprehensive fashion and at the scale of populations of
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Book chapters on the topic "Enhancers RNAs"

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Fladung, Matthias, Hely Häggman, and Suvi Sutela. "Application of RNAi technology in forest trees." In RNAi for plant improvement and protection. CABI, 2021. http://dx.doi.org/10.1079/9781789248890.0054.

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Abstract A diverse set of small RNAs is involved in the regulation of genome organization and gene expression in plants. These regulatory sRNAs play a central role for RNA in evolution and ontogeny in complex organisms, including forest tree species, providers of indispensable ecosystem services. RNA interference is a process that inhibits gene expression by double-stranded RNA and thus causes the degradation of target messenger RNA molecules. Targeted gene silencing by RNAi has been utilized in various crop plants in order to enhance their characteristics. For forest tree species, most of the successful RNAi modification has been conducted in poplar. Over the past 20 years, successful RNAi-mediated suppression of gene expression has been achieved with a variety of economically important traits. Moreover, the stability of RNAi-mediated transgene suppression has been confirmed in field-grown poplars. In this chapter, we describe examples of successful RNAi applications mainly in poplar but also provide some information about application of RNAi in pest control in forest tree species. Advantages and disadvantages of this technology with respect to the particular features of forest tree species will be discussed.
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Fladung, Matthias, Hely Häggman, and Suvi Sutela. "Application of RNAi technology in forest trees." In RNAi for plant improvement and protection. CABI, 2021. http://dx.doi.org/10.1079/9781789248890.0007.

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Abstract A diverse set of small RNAs is involved in the regulation of genome organization and gene expression in plants. These regulatory sRNAs play a central role for RNA in evolution and ontogeny in complex organisms, including forest tree species, providers of indispensable ecosystem services. RNA interference is a process that inhibits gene expression by double-stranded RNA and thus causes the degradation of target messenger RNA molecules. Targeted gene silencing by RNAi has been utilized in various crop plants in order to enhance their characteristics. For forest tree species, most of the successful RNAi modification has been conducted in poplar. Over the past 20 years, successful RNAi-mediated suppression of gene expression has been achieved with a variety of economically important traits. Moreover, the stability of RNAi-mediated transgene suppression has been confirmed in field-grown poplars. In this chapter, we describe examples of successful RNAi applications mainly in poplar but also provide some information about application of RNAi in pest control in forest tree species. Advantages and disadvantages of this technology with respect to the particular features of forest tree species will be discussed.
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de Schutter, Kristof, Olivier Christiaens, Clauvis Nji Tizi Taning, and Guy Smagghe. "Boosting dsRNA delivery in plant and insect cells with peptide- and polymer-based carriers: case-based current status and future perspectives." In RNAi for plant improvement and protection. CABI, 2021. http://dx.doi.org/10.1079/9781789248890.0102.

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Abstract Since the discovery of this naturally occurring endogenous regulatory and defence mechanism, RNA interference (RNAi) has been exploited as a powerful tool for functional genomic research. In addition, it has evolved as a promising candidate for a sustainable, specific and ecofriendly strategy for pest management and plant improvement. A key element in this technology is the efficient delivery of dsRNAs into the pest or plant tissues. While several examples using transgenic plants expressing the dsRNAs have proved the potential of this technology, nontransgenic approaches are investigated as alternatives, allowing flexibility and circumventing technical limitations of the transgenic approach. However, the efficacy of environmental RNAi is affected by several barriers, such as extracellular degradation of the dsRNA, inefficient internalization of the dsRNA in the cell and low endosomal escape into the cytoplasm, resulting in variable or low RNAi responses. In the medical field, carrier systems are commonly used to enhance RNA delivery and these systems are being rapidly adopted by the agricultural industry. Using four case studies, this chapter demonstrates the potential of carriers to improve the RNAi response in pest control for aquatic-living mosquito larvae and RNAi-resilient Lepidoptera and to cross the plant cell wall, allowing efficient environmental RNAi in plants.
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de Schutter, Kristof, Olivier Christiaens, Clauvis Nji Tizi Taning, and Guy Smagghe. "Boosting dsRNA delivery in plant and insect cells with peptide- and polymer-based carriers: case-based current status and future perspectives." In RNAi for plant improvement and protection. CABI, 2021. http://dx.doi.org/10.1079/9781789248890.0011.

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Abstract Since the discovery of this naturally occurring endogenous regulatory and defence mechanism, RNA interference (RNAi) has been exploited as a powerful tool for functional genomic research. In addition, it has evolved as a promising candidate for a sustainable, specific and ecofriendly strategy for pest management and plant improvement. A key element in this technology is the efficient delivery of dsRNAs into the pest or plant tissues. While several examples using transgenic plants expressing the dsRNAs have proved the potential of this technology, nontransgenic approaches are investigated as alternatives, allowing flexibility and circumventing technical limitations of the transgenic approach. However, the efficacy of environmental RNAi is affected by several barriers, such as extracellular degradation of the dsRNA, inefficient internalization of the dsRNA in the cell and low endosomal escape into the cytoplasm, resulting in variable or low RNAi responses. In the medical field, carrier systems are commonly used to enhance RNA delivery and these systems are being rapidly adopted by the agricultural industry. Using four case studies, this chapter demonstrates the potential of carriers to improve the RNAi response in pest control for aquatic-living mosquito larvae and RNAi-resilient Lepidoptera and to cross the plant cell wall, allowing efficient environmental RNAi in plants.
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Zou, Qingping, Ying Liang, Huaibing Luo, and Wenqiang Yu. "miRNA-Mediated RNAa by Targeting Enhancers." In RNA Activation. Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-4310-9_8.

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Allison, Karmel A., and Christopher K. Glass. "Macrophage Activation as a Model System for Understanding Enhancer Transcription and eRNA Function." In Long Noncoding RNAs. Springer Japan, 2015. http://dx.doi.org/10.1007/978-4-431-55576-6_12.

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Bialkowski, Lukasz, Kevin Van der Jeught, Dries Renmans, et al. "Adjuvant-Enhanced mRNA Vaccines." In RNA Vaccines. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-6481-9_11.

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Andersen, Morten Østergaard, and Jørgen Kjems. "RNA Interference Enhanced Implants." In Active Implants and Scaffolds for Tissue Regeneration. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/8415_2011_68.

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Broderick, Kate E., and Laurent M. Humeau. "Enhanced Delivery of DNA or RNA Vaccines by Electroporation." In RNA Vaccines. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-6481-9_12.

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Shibayama, Youtaro, Stephanie Fanucchi, and Musa M. Mhlanga. "Visualization of Enhancer-Derived Noncoding RNA." In Methods in Molecular Biology. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-4035-6_3.

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Conference papers on the topic "Enhancers RNAs"

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Hou, Tim Y., and William L. Kraus. "Abstract P1-05-02: Estrogen-regulated enhancer RNAs control enhancer assembly and function in breast cancer cells." In Abstracts: 2019 San Antonio Breast Cancer Symposium; December 10-14, 2019; San Antonio, Texas. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.sabcs19-p1-05-02.

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Firestein, Ron, Mark McCleland, Kathryn Mesh, and Florian Gnad. "Abstract 406: Enhancer templated RNAs as predictors of therapeutic response to epigenetic therapy." In Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-406.

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Zhang, Fan, Won-min Song, SiDe Li, et al. "Abstract PR06: The enhancer landscape involves a core noncoding RNA protein interaction network forC-MYCexpression." In Abstracts: AACR Special Conference on Noncoding RNAs and Cancer: Mechanisms to Medicines; December 4-7, 2015; Boston, MA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.nonrna15-pr06.

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Li, Zhiqian. "Enhanced RNAi efficiency of silkworm through overexpression of Ago2." In 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.95338.

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Guo, Yang Eric, and Richard Young. "Abstract A166: Biogenesis and regulatory functions of super-enhancer RNAs in cancer cells of the immune system." In Abstracts: CRI-CIMT-EATI-AACR Inaugural International Cancer Immunotherapy Conference: Translating Science into Survival; September 16-19, 2015; New York, NY. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/2326-6074.cricimteatiaacr15-a166.

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Lim, Zhining, and Braden J. Phillips. "An RNS-Enhanced Microprocessor Implementation of Public Key Cryptography." In 2007 41st Asilomar conference on Signals, Systems and Computers (ACSSC). IEEE, 2007. http://dx.doi.org/10.1109/acssc.2007.4487465.

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Palronik, Piotr, and Stanislaw J. Piestrak. "Design of a low-power RNS-enhanced arithmetic unit." In 2016 IEEE 7th Latin American Symposium on Circuits & Systems (LASCAS). IEEE, 2016. http://dx.doi.org/10.1109/lascas.2016.7451032.

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Azofeifa, Joseph, Joel Basken, Maria Lai, et al. "Abstract 4689: Co-treatment of MEKi and BRD4 inhibitors lead to synergistic repression of MYC-associated enhancer RNAs." In Proceedings: AACR Annual Meeting 2020; April 27-28, 2020 and June 22-24, 2020; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-4689.

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Fellmann, Christof, Thomas Hoffmann, Vaishali Sridhar, Barbara Hopfgartner, Dan Y. Lai, and Johannes Zuber. "Abstract 4273: An enhanced microRNA backbone for potent single-copy RNAi." In Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-4273.

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Subedi, Udaya. "RNAi mediated down-regulation of various genes enhances abiotic stress tolerance in alfalfa." In ASPB PLANT BIOLOGY 2020. ASPB, 2020. http://dx.doi.org/10.46678/pb.20.1052945.

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Reports on the topic "Enhancers RNAs"

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Weiss, Ron, and Liliana Wroblewska. An RNAi-enhanced Logic Circuit for Cancer Specific Detection and Destruction. Defense Technical Information Center, 2010. http://dx.doi.org/10.21236/ada542442.

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Weiss, Ron. An RNAi-Enhanced Logic Circuit for Cancer-Specific Detection and Destruction. Defense Technical Information Center, 2011. http://dx.doi.org/10.21236/ada553119.

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Weiss, Ron, Liliana Wroblewska, and Zhen Xie. An RNAi-Enhanced Logic Circuit for Cancer Specific Detection and Destruction. Defense Technical Information Center, 2013. http://dx.doi.org/10.21236/ada582947.

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Weiss, Ron, Liliana Wroblewska, and Zhen Xie. An RNAi-Enhanced Logic Circuit for Cancer Specific Detection and Destruction. Defense Technical Information Center, 2012. http://dx.doi.org/10.21236/ada567986.

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Loy, Duan S., Lyric Bartholomay, and D. L. Hank Harris. Injection of Double Stranded RNA Enhances Survival of Litopenaeus vannamei Challenged with White Spot Syndrome Virus. Iowa State University, 2012. http://dx.doi.org/10.31274/ans_air-180814-1051.

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